Author

Micheline Misrahi

Assistance Publique – Hôpitaux de ParisORCID 0000-0002-5379-8859Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Approach:benchmark study· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

"Genetics and the General Public" FFGH Ethics Working Group· 1 shared Abdelkader HeddariD· 1 shared Anne Cambon‐ThomseniD· 1 shared Bernard S. LópeziD· 1 shared Boris ChaumetteiD· 1 shared Célia CretolleiD· 1 shared Chloé Laeng· 1 shared David Heard· 1 shared

Activity by Year

2020-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

"Genetics and the General Public" FFGH Ethics Working Group

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJul 19, 2026

Knowledge and misconceptions of the French population regarding medical genetics: a survey of 3,000 respondents

Sandra Mercier, Francois Michael Petit, Micheline Misrahi…·"Genetics and the General Public" FFGH Ethics Working Group

This study surveys 3,000 French individuals to assess their knowledge and misconceptions about medical genetics, revealing limited understanding and significant gaps in awareness of genetic testing limitations and legal frameworks.

DOI 10.64898/2026.07.17.26358259

benchmark study

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GeneticsJournal of Medical GeneticsPeer-reviewedJun 1, 2020

A homozygous hypomorphic BRCA2 variant causes primary ovarian insufficiency without cancer or Fanconi anemia traits.

Sandrine Caburet, Abdelkader Heddar, Elodie Dardillac…·Micheline Misrahi

This study identifies a BRCA2 variant causing primary ovarian insufficiency without cancer or Fanconi anemia, showing residual HR function in patient cells.

47 citationstop 5%

humanwhole-exome sequencing

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